Pastuszak I, Szymona M
Acta Microbiol Pol A. 1975;8(3):131-9.
Seven Mycobacterium strains were grown statically on salts-glycerol-asparagine (Sauton) or on salts-glucose-glutamate (Sym) media. At desired time of incubation, the bacteria were washed with water, disintegrated with powdered corundum and in resulting cell-free extracts L-asparaginase activity was determined by the Conway method. The majority of experiments were performed on M. phlei which exhibited considerable rise in L-asparaginase activity with increasing age of the culture. This change did not occur on Sym medium because of Zn2+, which proved to abolish the effect of the enzyme induction in vivo but did not inhibit the activity in vitro. Addition of rifampicin to Sauton culture media resulted in a low enzyme level. Exogenous asparagine and glycerol were not indispensable for the enzyme synthesis and could be replaced by glutamate and glucose, respectively.
七株分枝杆菌菌株在盐-甘油-天冬酰胺(索顿)或盐-葡萄糖-谷氨酸(Sym)培养基上静置培养。在培养至所需时间时,用水洗涤细菌,用刚玉粉破碎,然后用康威法测定所得无细胞提取物中的L-天冬酰胺酶活性。大多数实验是在草分枝杆菌上进行的,随着培养时间的延长,该菌的L-天冬酰胺酶活性显著升高。在Sym培养基上未出现这种变化,因为锌离子可消除体内酶诱导的作用,但不抑制体外活性。在索顿培养基中添加利福平会导致酶水平降低。外源天冬酰胺和甘油对于酶的合成并非不可或缺,可分别用谷氨酸和葡萄糖替代。